Literature DB >> 1865578

Hypophosphatasia in an adult: a case report.

M Nangaku1, N Sato, K Sugano, F Takaku.   

Abstract

In this rare case of adult hypophosphatasia, no radiological abnormalities of the skeletal system could be detected even by dual energy X-ray absorptiometry. Severe dental caries was the sole clinical manifestation, indicating this case as an "odontohypophosphatasia". The levels of serum osteocalcin were low, which may be a useful biochemical marker to diagnose hypophosphatasia. Southern blot analyses of the genomic DNA revealed no gross abnormalities. Thus, hypophosphatasia in this patient was presumed to be caused by point mutations or small deletions. In a review of previous reports, an increased incidence among women was found.

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Year:  1991        PMID: 1865578     DOI: 10.2169/internalmedicine1962.30.47

Source DB:  PubMed          Journal:  Jpn J Med        ISSN: 0021-5120


  2 in total

1.  The Clinical Picture of Patients Suffering from Hypophosphatasia-A Rare Metabolic Disease of Many Faces.

Authors:  Izabela Michałus; Aneta Gawlik; Katarzyna Wieczorek-Szukała; Andrzej Lewiński
Journal:  Diagnostics (Basel)       Date:  2022-03-30

2.  Redox-Dependent Bone Alkaline Phosphatase Dysfunction Drives Part of the Complex Bone Phenotype in Mice Deficient for Memo1.

Authors:  Matthias B Moor; Suresh K Ramakrishnan; Finola Legrand; Silvia Dolder; Mark Siegrist; Fanny Durussel; Gabriel Centeno; Dmitri Firsov; Nancy E Hynes; Willy Hofstetter; Olivier Bonny
Journal:  JBMR Plus       Date:  2018-01-17
  2 in total

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